Shandong Qiaopai Group Co., Ltd. is one of 2168 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Shandong Qiaopai Group Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: MODEL TW SB, SCALP VEIN SET
1
Total
1
Cleared
0
Denied
Shandong Qiaopai Group Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Zibo, CN.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Shandong Qiaopai Group Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Shandong Qiaopai Group Co., Ltd.
1 devices